Telerehabilitation as an Alternative to Face-to-Face Rehabilitation After Total Hip Arthroplasty
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Exercise, Exercise.
- Who it may be relevant to
- Registry conditions: Total Hip Arthroplasty (THA). Basic parameters: 50 years — 80 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Turkey (Türkiye)
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Is Telerehabilitation a Good Alternative to Face-to-Face Rehabilitation Beyond Clinical Walls in Recovery After Total Hip Arthroplasty
Overview
The goal of this clinical trial is to learn if telerehabilitation in patients who had undergone total hip arthroplasty. The main questions it aims to answer are: * Does telerehabilitation improve the functional level of the participants? * Does telerehabilitation improve the locomotor performance of the participants? Researchers will compare telerehabilitation to face to face rehabilitation (traditional rehabilitation programme) to see if telerehabilitation works in total hip arthroplasty recovery. Participants will: * Attend physiotherapy and rehabilitation sessions supervised by a physiotherapist 2 days a week for 8 weeks. * Participate in assessments (before surgery and at 6 weeks and 12 weeks after surgery).
Interventions
- Other Exercise
exercise programme will be implemented via telerehabilitation - Other Exercise
exercise programme will be implemented via face-to-face
Primary outcome measures
- Functional level [Time frame: Assessments will be performed before surgery and at 6 weeks and 12 weeks after surgery.]
Secondary outcome measures (5)
- Pain intensity [Time frame: Assessments will be performed before surgery and at 6 weeks and 12 weeks after surgery.]
- Quality of life [Time frame: Assessments will be performed before surgery and at 6 weeks and 12 weeks after surgery.]
- Locomotor performance [Time frame: Assessments will be performed before surgery and at 6 weeks and 12 weeks after surgery.]
- Lower extremity muscle strength [Time frame: Assessments will be performed before surgery and at 6 weeks and 12 weeks after surgery.]
- Hip Joint Range of Motion (ROM) [Time frame: Assessments will be performed before surgery and at 6 weeks and 12 weeks after surgery.]
Eligibility criteria
Inclusion criteria
- Having hip arthroplasty surgery
- To be able to understand verbal and written information
- No cognitive impairment
- To be able to speak and understand Turkish
Exclusion criteria
- Having a neurological disease
- Having a psychiatric disorder
- Visual or hearing loss that cannot be corrected with any assistive device
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Single blind
- Primary purpose
- Treatment
Study locations
Turkey (Türkiye) · 1 center
- Burdur Mehmet Akif Ersoy University — Burdur
Identifiers
NCT: NCT06708884 · ErsoyU.22112024